EP0615542B1 - Fluessige waschmittel mit zitronensaeure, cellulase und bor-diol-komplex um proteolytisches enzym zu inhibieren - Google Patents

Fluessige waschmittel mit zitronensaeure, cellulase und bor-diol-komplex um proteolytisches enzym zu inhibieren Download PDF

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EP0615542B1
EP0615542B1 EP92925473A EP92925473A EP0615542B1 EP 0615542 B1 EP0615542 B1 EP 0615542B1 EP 92925473 A EP92925473 A EP 92925473A EP 92925473 A EP92925473 A EP 92925473A EP 0615542 B1 EP0615542 B1 EP 0615542B1
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alkyl
cellulase
acid
liquid laundry
detergent composition
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EP0615542A1 (de
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Stanton Lane Boyer
Tomothy Joseph Farwick
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Procter and Gamble Co
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Procter and Gamble Co
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    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38645—Preparations containing enzymes, e.g. protease or amylase containing cellulase
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16—Organic compounds
    • C11D3/38—Products with no well-defined composition, e.g. natural products
    • C11D3/386—Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38663—Stabilised liquid enzyme compositions

Definitions

  • This invention relates to liquid laundry detergent compositions containing anionic or nonionic surfactant, citric acid or a water-soluble salt thereof, proteolytic enzyme, cellulase, 1,2 propane diol (hereinafter also referred to as diol) and boric acid or its derivative (hereinafter also referred to as boric acid).
  • the compositions are prepared by adding the diol and boric acid to the composition before adding the citric acid/salt to the composition. This order of addition improves the stability of the cellulase in the presence of the proteolytic enzyme.
  • protease-containing liquid detergents A commonly encountered problem with protease-containing liquid detergents is the degradation of other enzymes in the composition by the proteolytic enzyme. The stability of the other enzyme upon storage and its performance can be impaired by the proteolytic enzyme.
  • boronic acid peptide boronic acid
  • peptide boronic acid is discussed as an inhibitor of trypsin-like serine proteases, especially in pharmaceuticals, in European Patent Application 0 293 881, Kettner et al., published December 7, 1988.
  • boric acid appears to complex with the citric acid/salt. It is believed that this adversely affects boric acid's function as a proteolytic enzyme inhibitor. The proteolytic enzyme then is free to degrade cellulase in the composition, rendering it less effective.
  • the extent to which the citric acid/salt complexes with a boric acid derivative is believed to be a function of the type of derivative employed in the composition.
  • boric acid as a proteolytic enzyme inhibitor can be increased by the addition of 1,2 propane diol. Without intending to be limited by theory, it is believed that a predominantly 1:1 molar boric/diol complex is formed which is capable of binding with the active site (serine) on the proteolytic enzyme and inhibiting it.
  • boric acid to liquid detergents containing citric acid/salt and 1,2 propane diol does not significantly improve cellulase stability in the presence of protease unless the boric acid and diol are added to the composition prior to the citric acid.
  • the boric/diol mixture is an effective protease inhibitor even in the presence of citric acid or a salt thereof. This minimizes degradation of the cellulase by the proteolytic enzyme. Upon dilution in water, such as under typical wash conditions, the proteolytic enzyme is no longer inhibited and can function to remove protease-sensitive stains from fabrics.
  • European Patent Application 0 381 262 discloses mixtures of proteolytic and lipolytic enzymes in a liquid medium.
  • the stability of lipolytic enzyme is said to be improved by the addition of a stabilizer system comprising boron compound and a polyol capable of reacting with it, whereby the polyol has a first binding constant of at least 500 l/mole and a second binding constant with the boron compound of at least 1000 l2/mole2.
  • German Patent 3 918 761 Weiss et al, published June 28, 1990, discloses a liquid enzyme concentrate which is said to be usable as a raw material solution for making liquid detergents and the like.
  • the concentrate contains hydrolase, propylene glycol and boric acid or its soluble salt.
  • the composition also contains a stabilization system comprised of glycerine, a boron compound and a carboxylic compound with 2-8 carbon compounds.
  • the present invention relates to a liquid laundry detergent composition
  • a liquid laundry detergent composition comprising, by weight:
  • the liquid laundry detergent compositions herein contain anionic or nonionic surfactant, or mixtures thereof, citric acid or a water-soluble salt thereof, 1,2 propane diol, boric acid or its derivative, proteolytic enzyme, cellulase, and water.
  • the compositions are prepared by adding the 1,2 propane diol and boric acid or its derivative to the composition before adding the citric acid or salt to the composition. This order of addition significantly increases the stability of the cellulase in the presence of the proteolytic enzyme.
  • compositions of the invention contain from 5 to 50, preferably 10 to 40, most preferably 12 to 30, weight % of anionic or nonionic surfactant. Mixtures of such surfactants are also contemplated herein. It is preferred that no significant amount of surfactant other than anionic and nonionic surfactants be included.
  • the preferred cellulase herein is denatured by alkyl sulfate and linear alkylbenzene sulfonate anionic surfactants.
  • Ethoxylated and sugar-based surfactants prevent such denaturing of the cellulase. It is therefore preferred that at least 25%, preferably at least 50%, more preferably at least 75%, by weight of the surfactant is an ethoxylated and/or sugar-based anionic or nonionic surfactant.
  • Preferred anionic surfactants herein include C12-C18 alkyl sulfates and C11-C13 linear alkylbenzene sulfonates for good cleaning performance, and C12-C18 alkyl sulfates ethoxylated with an average of from 1 to 6 moles of ethylene oxide per mole of alky sulfate for good cleaning and to minimize denaturing of the cellulase by alkyl sulfate and alkylbenzene sulfonate surfactants.
  • the nonionic surfactant is a condensation product of C10-C18 alcohol and between 2-20 (preferably 5 to 12) moles of ethylene oxide per mole of alcohol, or a polyhydroxy C12 ⁇ 18 (preferably C11 ⁇ 15) fatty acid amide.
  • the above and other surfactants useful herein are described in more detail hereinafter.
  • Alkyl ester sulfonate surfactants can be utilized in the invention. These are desirable because they can be made with renewable, non-petroleum resources. Preparation of the alkyl ester sulfonate surfactant component is according to known methods disclosed in the technical literature. For instance, linear esters of C8-C20 carboxylic acids can be sulfonated with gaseous SO3 according to "The Journal of the American Oil Chemists Society," 52 (1975), pp. 323-329. Suitable starting materials would include natural fatty substances as derived from tallow, palm, and coconut oils, etc.
  • the preferred alkyl ester sulfonate surfactant is of the structural formula: wherein R3 is a C8-C20 hydrocarbyl, preferably an alkyl, or combination thereof, R4 is a C1-C6 hydrocarbyl, preferably an alkyl, or combination thereof, and M is a soluble salt-forming cation.
  • Suitable salts include metal salts such as sodium, potassium, and lithium salts, and substituted or unsubstituted ammonium salts, such as methyl-, dimethyl, -trimethyl, and quaternary ammonium cations, e.g. tetramethyl-ammonium and dimethyl piperydinium, and cations derived from alkanolamines, e.g.
  • R3 is C10-C16 alkyl
  • R4 is methyl, ethyl or isopropyl.
  • methyl ester sulfonates wherein R3 is C14-C16 alkyl.
  • Alkyl sulfate surfactants are another type of anionic surfactant for use herein. Included are water soluble salts or acids of the formula ROSO3M wherein R preferably is a C10-C24 hydrocarbyl, preferably an alkyl or hydroxyalkyl having a C10-C20 alkyl component, more preferably a C12-C18 alkyl or hydroxyalkyl, and M is H or a cation, e.g., an alkali metal cation (e.g., sodium, potassium, lithium), substituted or unsubstituted ammonium cations such as methyl-, dimethyl-, and trimethyl ammonium and quaternary ammonium cations, e.g., tetramethyl-ammonium and dimethyl piperdinium, and cations derived from alkanolamines such as ethanolamine, diethanolamine, triethanolamine, and mixtures thereof, and the like. Typically, alkyl chains of C12
  • Alkyl alkoxylated sulfate surfactants are another category of useful anionic surfactant. These surfactants are water soluble salts or acids typically of the formula RO(A) m SO3M wherein R is an unsubstituted C10-C24 alkyl or hydroxyalkyl group having a C10-C24 alkyl component, preferably a C12-C20 alkyl or hydroxyalkyl, more preferably C12-C18 alkyl or hydroxyalkyl, A is an ethoxy (preferred) or propoxy unit, m is greater than zero, typically between about 0.5 and about 20, more preferably between about 1 and about 4, and M is H or a cation which can be, for example, a metal cation (e.g., sodium, potassium, lithium, calcium, magnesium, etc.), ammonium or substituted-ammonium cation.
  • R is an unsubstituted C10-C24 alkyl or hydroxyalkyl group having a C
  • substituted ammonium cations include methyl-, dimethyl-, trimethyl-ammonium and quaternary ammonium cations, such as tetramethyl-ammonium, dimethyl piperydinium and cations derived from alkanolamines, e.g. monoethanolamine, diethanolamine, and triethanolamine, and mixtures thereof.
  • Exemplary surfactants are C12-C18 alkyl polyethoxylate (1.0) sulfate, C12-C18 alkyl polyethoxylate (2.25) sulfate, C12-C18 alkyl polyethoxylate (3.0) sulfate, and C12-C18 alkyl polyethoxylate (4.0) sulfate, wherein M is conveniently selected from sodium and potassium.
  • Alkyl ethoxy carboxylate surfactants of this invention are of the formula RO(CH2CH2O) x CH2COO ⁇ M+ wherein R is a C8 to C18 (preferably C12-C18) alkyl group, x is a number averaging from about 1 to 15, (preferably about 2 to 6), and M is an alkali metal or an alkaline earth metal cation (preferably sodium or potassium).
  • R is a C8 to C18 (preferably C12-C18) alkyl group
  • x is a number averaging from about 1 to 15, (preferably about 2 to 6)
  • M is an alkali metal or an alkaline earth metal cation (preferably sodium or potassium).
  • the alkyl chain having from about 8 to about 18 carbon atoms can be drived from fatty alcohols, olefins, etc. Normally, and preferably, the alkyl chain will be a mixture of alkyl chains. However, pure alkyl chains can be used.
  • the alkyl chain is desirably a straight saturated alkyl chain, but it may also be a branched and/or unsaturated alkyl chain.
  • These surfactants and methods of making them are described in European Patent Application 90305468.2, published November 28, 1990, incorporated herein by reference.
  • anionic surfactants that can be included in the compositions are the salts (including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts) of soap, C9-C20 linear alkylbenzene sulphonates, C8-C22 primary or secondary alkane sulphonates, C8-C24 olefin sulphonates, sulphonated polycarboxylic acids prepared by sulphonation of the pyrolyzed product of alkaline earth metal citrates, e.g., as described in British Patent Specification No.
  • salts including, for example, sodium, potassium, ammonium, and substituted ammonium salts such as mono-, di- and triethanolamine salts
  • C9-C20 linear alkylbenzene sulphonates C8-C22 primary or secondary alkane sulphonates
  • C8-C24 olefin sulphonates C8-C24
  • alkyl glycerol sulfonates 1,082,179, alkyl glycerol sulfonates, fatty acyl glycerol sulfonates, fatty oleyl glycerol sulfates, alkyl phenol ethylene oxide ether sulfates, paraffin sulfonates, alkyl phosphates, isothionates such as the acyl isothionates, N-acyl taurates, fatty acid amides of methyl tauride, alkyl succinamates and sulfosuccinates, monoesters of sulfosuccinate (especially saturated and unsaturated C12-C18 monoesters) diesters of sulfosuccinate (especially saturated and unsaturated C6-C14 diesters), N-acyl sarcosinates, sulfates of alkylpolysaccharides such as the sulfates of alkylpol
  • Resin acids and hydrogenated resin acids are also suitable, such as rosin, hydrogenated rosin, and resin acids and hydrogenated resin acids present in or derived from tall oil. Further examples are given in "Surface Active Agents and Detergents" (Vol. I and II by Schwartz, Perry and Berch). A variety of such surfactants are also generally disclosed in U.S. Patent 3,929,678, issued December 30, 1975 to Laughlin, et al. at Column 23, line 58 through Column 29, line 23.
  • Suitable nonionic detergent surfactants are generally disclosed in U.S. Patent 3,929,678, Laughlin et al., issued December 30, 1975, at column 13, line 14 through column 16, line 6. Exemplary, non-limiting classes of useful nonionic surfactants are listed below.
  • R' can be, for example, N-methyl, N-ethyl, N-propyl, N-isopropyl, N-butyl, N-2-hydroxy ethyl, or N-2-hydroxy propyl.
  • R2-CO-N ⁇ can be, for example, cocamide, stearamide, oleamide, lauramide, myristamide, capricamide, palmitamide, tallowamide, etc.
  • Z can be 1-deoxyglucityl, 2-deoxyfructityl, 1-deoxymaltityl, 1-deoxylactityl, 1-deoxygalactityl, 1-deoxymannityl, 1-deoxymaltotriotityl, etc.
  • polyhydroxy fatty acid amides are known in the art. In general, they can be made by reacting an alkyl amine with a reducing sugar in a reductive amination reaction to form a corresponding N-alkyl polyhydroxyamine, and then reacting the N-alkyl polyhydroxyamine with a fatty aliphatic ester or triglyceride in a condensation/amidation step to form the N-alkyl, N-polyhydroxy fatty acid amide product.
  • Processes for making compositions containing polyhydroxy fatty acid amides are disclosed, for example, in G.B. Patent Specification 809,060, published February 18, 1959, U.S. Patent 2,965,576, issued December 20, 1960 to E. R. Wilson, and U.S. Patent 2,703,798, Anthony M. Schwartz, issued March 8, 1955, and U.S. Patent 1,985,424, issued December 25, 1934 to Piggott.
  • compositions herein further contain from 1 to 10, preferably 1.5 to 8, weight % of citric acid.
  • Water-soluble salts of citric acid are also useful in the liquid detergent compositions herein.
  • the liquid detergent compositions herein contain a mixture of 1,2 propane diol and boric acid or its derivative.
  • the final concentration of boric acid or its derivative in the detergent composition is between 0.5 and 5% by weight and the final concentration of 1,2 propanediol is between 1 and 20% by weight.
  • the concentration of boric acid or its derivative in the composition is between 1 and 4 weight %, and most preferably between 1.5 and 3 weight %.
  • the concentration of diol in the composition is preferably between 3 and 15, most preferably between 5 and 12, weight %.
  • the diol/boric weight ratio is preferably between 1:1 and 20:1, more preferably between 2:1 and 10:1. This insures sufficient diol to form the preferred 1:1 molar diol/boric complex, while providing additional diol to aid in the dissolution of other ingredients during processing and storage.
  • Suitable boric acid derivatives include borax, boric oxide, polyborates, orthoborates, pyroborates, and metaborates, or mixtures thereof.
  • Preferred compounds are the alkali salts of boric acid, such as sodium borate, and amine salts thereof, such as the monoethanol salt of boric acid. These salts can be formed in the formulation by in-situ neutralization of boric acid with an appropriate alkali or amine.
  • the liquid detergent compositions herein also contain from 0.0001 to 1.0, preferably 0.0005 to 0.3, most preferably 0.002 to 0.1, weight % of active proteolytic enzyme. Mixtures of proteolytic enzyme are also included.
  • the proteolytic enzyme can be of animal, vegetable or microorganism (preferred) origin. More preferred is serine proteolytic enzyme of bacterial origin. Purified or nonpurified forms of this enzyme can be used. Proteolytic enzymes produced by chemically or genetically modified mutants are included. Particularly preferred is bacterial serine proteolytic enzyme obtained from Bacillus subtilis and/or Bacillus licheniformis .
  • Suitable proteolytic enzymes include Alcalase®, Esperase®, Savinase®, Maxatase®, Maxacal®, Maxapem 15®, and subtilisin BPN and BPN', which are commercially available.
  • Preferred proteolytic enzymes are also modified bacterial serine proteases, such as those described in European Patent Application Serial Number 87 303761.8, filed April 28, 1987 (particularly pages 17, 24 and 98), particularly "Protease B" therein, and in European Patent Application 199,404, Venegas, published October 29, 1986, which refers to a modified bacterial serine proteolytic enzyme called "Protease A" therein.
  • the third essential ingredient in the present liquid compositions is a cellulase enzyme. It can be a bacterial or fungal cellulase.
  • the amount of cellulase used in the composition varies according to the type of cellulase and the use intended. In general, from 0.0001 to 1.0, more preferably 0.0002 to 0.5, weight % on an active basis of the cellulase is used. Preferably, the cellulase will have a pH optimum of between 5 and 9.5.
  • the level of the cellulase is such that the amount of enzyme protein to be delivered in the wash solution is preferably from 0.005 to 40 mg/liter of wash solution, more preferably 0.01 to 10 mg/liter of wash solution.
  • Suitable cellulases are disclosed in U.S. Patent 4,435,307, Barbesgaard et al., issued March 6, 1984, which discloses fungal cellulase produced from Humicola insolens . Suitable cellulases are also disclosed in GB-A-2.075.028, GB-A-2.095.275 and DE-OS-2.247.832.
  • cellulases examples include cellulases produced by a strain of Humicola insolens (Humicola grisea var. thermoidea ), particularly the Humicola strain DSM 1800, and cellulases produced by a fungus of Bacillus N or a cellulase 212-producing fungus belonging to the genus Aeromonas , and cellulase extracted from the hepatopancreas of a marine mollusc (Dolabella Auricula Solander).
  • One CMCase unit is defined as the amount of enzyme which forms per minute an amount of reducing carbohydrate equivalent to 10 ⁇ 6 mole of glucose, in the above-described conditions.
  • a useful range of cellulase activity in the present context is from 0.01 to 1360, preferably from 0.1 to 140 CMCase activity units/gram of detergent composition.
  • a preferred cellulase herein consists essentially of a homogenous endoglucanase component which is immunoreactive with an antibody raised against a highly purified 43 kD endoglucanase derived from Humicola insolens , DSM 1800, or which is homologous to said 43 kD endoglucanase.
  • the endoglucanase component preferably has an endoglucanase activity of at least 50 CMC-endoase units/mg of protein, more preferably at least 60 CMC-endoase units/mg of total protein, in particular at least 90 CMC-endoase units/mg of total protein, and most preferably at least 100 CMC-endoase units/mg of total protein.
  • the endoglucanase component preferably has an isoelectric point of 5.1.
  • compositions contain from 10% to 75%, preferably from 25% to 60%, by weight of water.
  • the composition may contain from 0 to 50, more preferably 2 to 30, most preferably 3 to 15, weight percent of other detergency builders. Inorganic as well as organic builders can be used.
  • Inorganic detergency builders include, but are not limited to, the alkali metal, ammonium and alkanolammonium salts of polyphosphates (exemplified by the tripolyphosphates, pyrophosphates, and glassy polymeric meta-phosphates), phosphonates, phytic acid, silicates, carbonates (including bicarbonates and sesquicarbonates), sulphates, and aluminosilicates.
  • Organic detergent builders preferred for the purposes of the present invention include a wide variety of polycarboxylate compounds.
  • polycarboxylate refers to compounds having a plurality of carboxylate groups, preferably at least two carboxylates.
  • Polycarboxylate builder can generally be added to the composition in acid form, but can also be added in the form of a neutralized salt.
  • alkali metals such as sodium, potassium, and lithium, or alkanolammonium salts are preferred.
  • polycarboxylate builders include a variety of categories of useful materials.
  • One important category of polycarboxylate builders encompasses the ether polycarboxylates.
  • a number of ether polycarboxylates have been disclosed for use as detergent builders.
  • Examples of useful ether polycarboxylates include oxydisuccinate, as disclosed in Berg, U.S. Patent 3,128,287, issued April 7, 1964, and Lamberti et al., U.S. Patent 3,635,830, issued January 18, 1972.
  • Still other ether polycarboxylates include copolymers of maleic anhydride with ethylene or vinyl methyl ether, 1, 3, 5-trihydroxy benzene-2, 4, 6-trisulphonic acid, and carboxymethyloxysuccinic acid.
  • Organic polycarboxylate builders also include the various alkali metal, ammonium and substituted ammonium salts of polyacetic acids. Examples include the sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediamine tetraacetic acid, and nitrilotriacetic acid.
  • polycarboxylates such as mellitic acid, succinic acid, oxydisuccinic acid, polymaleic acid, benzene 1,3,5-tricarboxylic acid, and carboxymethyloxysuccinic acid; and soluble salts thereof.
  • carboxylate builders include the carboxylated carbohydrates disclosed in U.S. Patent 3,723,322, Diehl, issued March 28, 1973.
  • succinic acid builders include the C5-C20 alkyl succinic acids and salts thereof.
  • a particularly preferred compound of this type is dodecenylsuccinic acid.
  • Alkyl succinic acids typically are of the general formula R-CH(COOH)CH2(COOH) i.e., derivatives of succinic acid, wherein R is hydrocarbon, e.g., C10-C20 alkyl or alkenyl, preferably C12-C16 or wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, all as described in the above-mentioned patents.
  • R is hydrocarbon, e.g., C10-C20 alkyl or alkenyl, preferably C12-C16 or wherein R may be substituted with hydroxyl, sulfo, sulfoxy or sulfone substituents, all as described in the above-mentioned patents.
  • the succinate builders are preferably used in the form of their water-soluble salts, including the sodium, potassium, ammonium and alkanolammonium salts.
  • succinate builders include: laurylsuccinate, myristylsuccinate, palmitylsuccinate, 2-dodecenylsuccinate (preferred), 2-pentadecenylsuccinate, and the like. Laurylsuccinates are the preferred builders of this group, and are described in European Patent Application 86200690.5/0,200,263, published November 5, 1986.
  • useful builders also include sodium and potassium carboxymethyloxymalonate, carboxymethyloxysuccinate, cis-cyclohexane-hexacarboxylate, cis-cyclopentane-tetracarboxylate, water-soluble polyacrylates (these polyacrylates having molecular weights to above about 2,000 can also be effecitvly utilized as dispersants), and the copolymers of maleic anhydride with vinyl methyl ether or ethylene.
  • polyacetal carboxylates are the polyacetal carboxylates disclosed in U.S. Patent 4,144,226, Crutchfield et al., issued March 13, 1979. These polyacetal carboxylates can be prepared by bringing together, under polymerization conditions, an ester of glyoxylic acid and a polymerization initiator. The resulting polyacetal carboxylate ester is then attached to chemically stable end groups to stabilize the polyacetal carboxylate against rapid depolymerization in alkaline solution, converted to the corresponding salt, and added to a surfactant.
  • Polycarboxylate builders are also disclosed in U.S. Patent 3,308,067, Diehl, issued March 7, 1967. Such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylenemalonic acid.
  • Preferred polycarboxylate builders for use herein having the general formula: CH(A)(COOX)-CH(COOX)-O-CH(COOX)-CH(COOX)(B) wherein A is hydroxyl; B is hydrogen or -O-CH(COOX)-CH2(COOX); and X is hydrogen or a salt-forming cation. If B is H, then the compound is tartrate monosuccinic acid (TMS) and its water-soluble salts. It is preferred that the above alphahydroxy acid (TMS) be mixed with tartrate disuccinate (TDS) represented by the above chemical structure wherein A is H and B is O-CH(COOX)-CH2(COOX).
  • These builders are disclosed in U.S. Patent 4,663,071, issued to Bush et al., on May 5, 1987.
  • organic builders known in the art can also be used.
  • monocarboxylic acids, and soluble salts thereof, having long chain hydrocarbyls can be utilized. These would include materials generally referred to as "soaps.” Chain lengths of C10-C20 are typically utilized.
  • the hydrocarbyls can be saturated or unsaturated.
  • compositions herein A wide variety of other ingredients useful in detergent compositions can be included in the compositions herein, including other active ingredients, other enzymes, soil release agents, soil suspending agents, brighteners, suds suppressors, carriers, hydrotropes, processing aids, dyes or pigments, solvents, bleaches, bleach activators, etc.
  • the liquid detergent compositions can contain other solvents such as low molecular weight primary or secondary alcohols exemplified by methanol, ethanol, propanol, and isopropanol.
  • Monohydric alcohols are preferred for solubilizing surfactant, but polyols such as those containing from 2 to about 6 carbon atoms and from 2 to about 6 hydroxy groups (e.g., ethylene glycol, and glycerine), can also be used.
  • liquid laundry detergent compositions herein are preferably formulated such that they have a pH in a 10% solution in water at 20°C of between 6.5 and 11.0, preferably 7.0 to 9.5.
  • Techniques for controlling pH at recommended usage levels include the use of buffers, alkalis, acids, etc., and are well known to those skilled in the art.
  • concentrated liquid detergent compositions Preferred herein are concentrated liquid detergent compositions. By “concentrated” is meant that these compositions will deliver to the wash the same amount of active ingredients at a reduced dosage.
  • Typical regular dosage of heavy duty liquids is 118 milliliters in the U.S. (about 1/2 cup) and 180 milliliters in Europe.
  • Concentrated heavy duty liquids herein contain about 10 to 100 weight % more active ingredients than regular heavy duty liquids, and are dosed at less than 1/2 cup depending upon their active levels. This invention becomes even more useful in concentrated formulations because there are more actives to interfere with enzyme performance.
  • Preferred are heavy duty liquid laundry detergent compositions with from 30 to 90, preferably 40 to 80, most preferably 50 to 70, weight % of active ingredients.
  • Example 2-6 are compositions of the present invention. Comparative Example 1 differs from Example 2 in that boric acid is added to the composition of Example 1 after the citric acid. In the table, the following abbreviations are used.
  • C45E 2.25 S is C14 ⁇ 15 alkyl polyethoxylate (2.25) sulfonic acid C23E 6.5
  • T is C12 ⁇ 13 alkyl ethoxylate (6.5), topped to remove unexthoxylated and monoethoxylated alcohols
  • MEA is monoethanolamine
  • Glucamide is C12 ⁇ 14 alkyl N-methyl glucamide
  • TEPA-E15 ⁇ 18 is tetraethylene pentaimine ethoxylated with 15-18 moles (avg.) of ethylene oxide at each hydrogen site on each nitrogen
  • Fatty acid is C12 ⁇ 14 fatty acid
  • NaTS is sodium tartrate mono- and di-succinate (80:20 mix)
  • Na Formate is sodium formate
  • Ca Formate is calcium formate
  • Protease is Protease B (34g/L) as described above Cellulase consists essentially of 43 kD endoglucanse described in PCT International Publication Number WO 91/17243
  • Patent 4,968,451 Ingredient Ex.1 Ex.2 Ex.3 Ex.4 Ex.5 Ex.6 C45E 2.25 S 14.92 14.92 16.90 16.40 19.90 21.00 Ethanol 3.60 3.60 3.60 2.88 3.60 5.00 C23E 6.5 T 0.85 0.85 2.00 1.64 0.85 0.00 MEA 2.30 2.30 3.50 2.80 2.30 3.50 Na Formate 0.24 0.24 0.30 0.24 0.24 0.45 Brightener 0.10 0.10 0.10 0.076 0.10 0.12 C24 Glucamide 4.98 4.98 3.20 0.00 0.00 7.00 1,2 Propane diol 10.00 10.00 10.00 8.00 10.00 7.00 NaTS 3.06 3.06 2.10 1.60 3.06 4.00 Boric Acid 2.50* 2.50 2.50 2.00 2.50 2.00 NaOH 2.80 2.80 2.51 2.01 2.80 3.10 Fatty Acid 2.30 2.30 1.25 2.00 2.30 3.00 Citric Acid 2.91 2.91 2.60 2.08 2.91 3.80 Ca Formate 0.09 0.09 0.09 0.07 0.09 0.00 TEPA-E15 ⁇
  • compositions of Examples 1, 2, 3 and 5 are evaluated for stability of the cellulase, measured as a percent of the initial performance provided by the cellulase in the composition, after storage at the indicated temperatures and times.
  • aged cotton fabrics are washed using the test compositions, tumble dried in an automatic dryer (which is preferred over line drying) and then visually graded by a panel of experts, after multiple wash/dry cycles, for restoration of fabric appearance.
  • the results are as follows.
  • Example 1 2 50% 50% 5 10% 10%
  • Example 2 2 - 90% 4 80% 50% 8 75% 75%
  • Example 5 2 75% - 4 80% 65% 8 100% 65%
  • Example 3** 4 - 40% **Made in a much larger quantity than Examples 1, 2 and 5.

Claims (7)

  1. Flüssige Wäschewaschmittelzusammensetzung, dadurch gekennzeichnet, daß sie, auf Gewichtsbasis,
    a. 5 bis 50%, vorzugsweise 10 bis 40%, eines anionischen oder nichtionischen Tensids, wobei mindestens 25%, vorzugsweise mindestens 50% hiervon ein ethoxyliertes Tensid oder ein Tensid auf Zuckerbasis sind;
    b. 1 bis 10%, vorzugsweise 1,5 bis 8%, Zitronensaure oder ein wasserlösliches Salz hiervon;
    c. 1 bis 20%, vorzugsweise 5 bis 12%, 1,2-Propandiol;
    d. 0,5 bis 5%, vorzugsweise 1,5 bis 3%, Borsäure oder dessen Derivat;
    e. 0,0001 bis 1,0%, vorzugsweise 0,002 bis 0,1%, eines aktiven proteolytischen Enzyms;
    f. 0,0001 bis 1,0%, vorzugsweise 0,0002 bis 0,5%, eines aktiven Cellulaseenzyms; und
    g. 10 bis 75% Wasser;
    umfaßt, wobei die Zusammensetzung in der Weise hergestellt wird, daß das 1,2-Propandiol und Borsäure oder dessen Derivat zu der Zusammensetzung gegeben werden, bevor die Zitronensäure oder ein Salz hiervon zu der Zusammensetzung gegeben wird.
  2. Flüssige Waschmittelzusammensetzung nach Anspruch 1, wobei das anionische Tensid ein C₁₂- bis C₁₈-Alkylsulfat, ein C₁₂- bis C₁₈-Alkylsulfat, das durchschnittlich mit 1 bis 6 Molen Ethylenoxid pro Mol Alkylsulfat ethoxyliert ist, oder ein lineares C₁₁ - bis C₁₃-Alkylbenzolsulfonat oder eine Mischung hiervon ist, und das nichtionische Tensid ein Kondensationsprodukt aus einem C₁₀-C₁₈-Alkohol und zwischen 2 und 20 Molen Ethylenoxid pro Mol Alkohol oder ein Polyhydroxy-C₁₂-C₁₈-Fettsäureamid ist.
  3. Flüssige Waschmittelzusammensetzung nach Anspruch 1 oder 2, wobei das Gewichtsverhältnis von 1,2-Propandiol zu Borsäure oder dessen Derivat zwischen 2:1 und 10:1 liegt.
  4. Flüssige Waschmittelzusammensetzung nach mindestens einem der vorangehenden Ansprüche, wobei die Cellulase im wesentlichen aus einer homogenen Endoglucanasekomponente besteht, welche mit einem gegenüber einer hochgereinigten 43 kD Endoglucanase, die von Humicola insolens, DSM 1800, abgeleitet ist, gebildeten Antikörper immunoreaktiv ist, oder welche zu der 43 kD Endoglucanase homolog ist.
  5. Flüssige Waschmittelzusammensetzung nach Anspruch 4, wobei die Endoglucanasekomponente eine Endoglucanaseaktivität von mindestens 50 CMC-Endoaseeinheiten/mg Protein aufweist.
  6. Flüssige Waschmittelzusammensetzung nach Anspruch 4 oder 5, wobei die Endoglucanasekomponente einen isoelektrischen Punkt von 5,1 aufweist.
  7. Flüssige Waschmittelzusammensetzung nach mindestens einem der vorangehenden Ansprüche mit einem pH in einer 10%-igen Lösung in Wasser bei 20° C zwischen 7,0 und 9,5.
EP92925473A 1991-12-04 1992-12-01 Fluessige waschmittel mit zitronensaeure, cellulase und bor-diol-komplex um proteolytisches enzym zu inhibieren Expired - Lifetime EP0615542B1 (de)

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US803310 1985-12-02
US80331091A 1991-12-04 1991-12-04
PCT/US1992/010363 WO1993011215A1 (en) 1991-12-04 1992-12-01 Liquid laundry detergents with citric acid, cellulase, and boric-diol complex to inhibit proteolytic enzyme

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CA2124788C (en) 1998-02-10
EP0615542A1 (de) 1994-09-21
ES2076794T3 (es) 1995-11-01
WO1993011215A1 (en) 1993-06-10
JP3244700B2 (ja) 2002-01-07
CA2124788A1 (en) 1993-06-10
CN1075331A (zh) 1993-08-18
DE69204472T2 (de) 1996-05-02
AU3151293A (en) 1993-06-28
US5476608A (en) 1995-12-19
MX9206992A (es) 1993-06-01
PH31148A (en) 1998-03-20
JPH07501574A (ja) 1995-02-16
TW232026B (de) 1994-10-11
CN1040019C (zh) 1998-09-30
DE69204472D1 (de) 1995-10-05

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